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2007•Magnetic Resonance in ChemistryRequires access

1H and 13C NMR spectra of C‐6 and C‐9 substituted 3‐azabicyclco[3.3.1]nonanes

Kirsten J. Goodall, Margaret A. Brimble, David Barker

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Abstract

The 1H and 13C NMR data for 3-azabicyclo[3.3.1]nonanes with OH and OMe substituents at C-6 and C-9 were measured using 1D (DEPT) and 2D (COSY, HSQC, HMBC, NOESY) experiments. Comparison of this NMR data illustrates the effects of stereochemistry and substitution at these positions.

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What this paper is about

The 1H and 13C NMR data for 3-azabicyclo[3.3.1]nonanes with OH and OMe substituents at C-6 and C-9 were measured using 1D (DEPT) and 2D (COSY, HSQC, HMBC, NOESY) experiments. Comparison of this NMR data illustrates the effects of stereochemistry and substitution at these positions.

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Available abstract

The 1H and 13C NMR data for 3-azabicyclo[3.3.1]nonanes with OH and OMe substituents at C-6 and C-9 were measured using 1D (DEPT) and 2D (COSY, HSQC, HMBC, NOESY) experiments. Comparison of this NMR data illustrates the effects of stereochemistry and substitution at these positions.

Key concepts: Chemistry, DEPT, Two-dimensional nuclear magnetic resonance spectroscopy, Heteronuclear single quantum coherence spectroscopy, Carbon-13 NMR, Stereochemistry, NMR spectra database, Spectral line

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1H and 13C NMR spectra of C‐6 and C‐9 substituted 3‐azabicyclco[3.3.1]nonanes — Research Paper | ScholarLens